(Q45059176)

English

Functional allelic heterogeneity and pleiotropy of a repeat polymorphism in tyrosine hydroxylase: prediction of catecholamines and response to stress in twins

scientific article published on 14 September 2004

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scholarly article

1 reference

Europe PubMed Central

9 December 2017

Functional allelic heterogeneity and pleiotropy of a repeat polymorphism in tyrosine hydroxylase: prediction of catecholamines and response to stress in twins (English)

1 reference

Europe PubMed Central

9 December 2017

1 reference

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Jennifer Wessel

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Jennifer Wessel

3

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Laurent Taupenot

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Laurent Taupenot

6

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author name string

Lian Zhang

1

1 reference

Europe PubMed Central

9 December 2017

Fangwen Rao

2

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Europe PubMed Central

9 December 2017

Brian P Kennedy

4

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Europe PubMed Central

9 December 2017

Brinda K Rana

5

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Europe PubMed Central

9 December 2017

Elizabeth O Lillie

7

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Europe PubMed Central

9 December 2017

Myles Cockburn

8

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Europe PubMed Central

9 December 2017

Nicholas J Schork

9

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Europe PubMed Central

9 December 2017

Michael G Ziegler

10

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Europe PubMed Central

9 December 2017

Daniel T O'Connor

11

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9 December 2017

publication date

14 September 2004

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Europe PubMed Central

9 December 2017

Physiological Genomics

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Europe PubMed Central

9 December 2017

19

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Europe PubMed Central

9 December 2017

3

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9 December 2017

277-291

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Europe PubMed Central

9 December 2017

Quantitative effects on gene silencing by allelic variation at a tetranucleotide microsatellite

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00151.2004

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Multipoint quantitative-trait linkage analysis in general pedigrees

1 reference

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Classical twin studies and beyond

1 reference

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Genetic manipulation of noradrenergic neurons.

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Physical mapping of autonomic/sympathetic candidate genetic loci for hypertension in the human genome: a somatic cell radiation hybrid library approach

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The occurrence of chronic disease and other conditions in a large population-based cohort of native Californian twins

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Genetic analysis of the age at menopause by using estimating equations and Bayesian random effects models.

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Base-calling of automated sequencer traces using phred. II. Error probabilities

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Base-calling of automated sequencer traces using phred. I. Accuracy assessment

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The NHLBI twin study of cardiovascular disease risk factors: methodology and summary of results

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Catecholamine biosynthesis and physiological regulation in neuroendocrine cells

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Structural Insight into the Aromatic Amino Acid Hydroxylases and Their Disease-Related Mutant Forms

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Plasma epinephrine levels in hypertension and across gender and ethnicity

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Crystal structure of tyrosine hydroxylase with bound cofactor analogue and iron at 2.3 A resolution: self-hydroxylation of Phe300 and the pterin-binding site

1 reference

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Consed: a graphical tool for sequence finishing

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A single human gene encoding multiple tyrosine hydroxylases with different predicted functional characteristics

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Beta2-adrenergic receptor polymorphisms at codon 16, cardiovascular phenotypes and essential hypertension in whites and African Americans

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A more sensitive and specific radioenzymatic assay for catecholamines

1 reference

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An association of the polymorphic repeat of tetranucleotide (TCAT) in the first intron of the human tyrosine hydroxylase gene with schizophrenia in a Japanese sample

1 reference

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21 January 2018

Initial sequencing and analysis of the human genome

1 reference

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21 January 2018

A tetranucleotide polymorphic microsatellite, located in the first intron of the tyrosine hydroxylase gene, acts as a transcription regulatory element in vitro

1 reference

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21 January 2018

Cardiovascular reactivity to the cold pressor test as a predictor of hypertension

1 reference

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PolyPhred: automating the detection and genotyping of single nucleotide substitutions using fluorescence-based resequencing

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Heredity and the autonomic nervous system in human hypertension

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Early decline in the catecholamine release-inhibitory peptide catestatin in humans at genetic risk of hypertension

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Isolation and characterization of the human tyrosine hydroxylase gene: identification of 5' alternative splice sites responsible for multiple mRNAs

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Autonomic function in hypertension. Are there racial differences?

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Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome

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The future of genetic studies of complex human diseases

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Stress-triggered activation of gene expression in catecholaminergic systems: dynamics of transcriptional events

1 reference

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21 January 2018

Cardiovascular haemodynamic response to repeated mental stress in normotensive subjects at genetic risk of hypertension: evidence of enhanced reactivity, blunted adaptation, and delayed recovery

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00151.2004

21 January 2018

Toward a causal model of cardiovascular responses to stress and the development of cardiovascular disease

1 reference

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Power of linkage versus association analysis of quantitative traits, by use of variance-components models, for sibship data

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00151.2004

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Positive association of tyrosine hydroxylase microsatellite marker to essential hypertension.

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00151.2004

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Dissecting the genetic architecture of the cardiovascular and renal stress response

1 reference

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Effect of chronic cold exposure on tyrosine hydroxylase mRNA in rat adrenal gland.

1 reference

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Chromogranin A in human hypertension. Influence of heredity

1 reference

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Association of DNA polymorphism in the first intron of the tyrosine hydroxylase gene with disturbances of the catecholaminergic system in schizophrenia

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00151.2004

21 January 2018

Cardiovascular reactivity and development of preclinical and clinical disease states

1 reference

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Initial sequencing and comparative analysis of the mouse genome

1 reference

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Both rare and common polymorphisms contribute functional variation at CHGA, a regulator of catecholamine physiology

1 reference

https://api.crossref.org/works/10.1152%2FPHYSIOLGENOMICS.00151.2004

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Linkage between tyrosine hydroxylase gene and affective disorder cannot be excluded in two of six pedigrees

1 reference

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Association of manic-depressive illness with tyrosine hydroxylase microsatellite marker

1 reference

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21 January 2018

Identifiers

10.1152/PHYSIOLGENOMICS.00151.2004

1 reference

Europe PubMed Central

9 December 2017

1 reference

Europe PubMed Central

9 December 2017

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